Regulatory Affairs Data & Technology Project Manager
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About this opportunity
#LI-HybridPrimary Location: London, United Kingdom (for candidates residing within 50 miles of the office)Other Locations: Remote, United Kingdom (UK based candidates living more than 50 miles from the office)Relocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Imagine shaping the future of Regulatory Affairs technology at a global scale. As the Regulatory Affairs Data & Technology Project Manager, you will play a pivotal role in driving the Regulatory Affairs Technology Roadmap, ensuring critical initiatives stay on track, on budget, and aligned to business priorities. Working across Regulatory Affairs, Data, Digital & Information Technology, and Technology teams, you will bring clarity to complex portfolios, connect stakeholders around shared goals, and help deliver innovative technology solutions that accelerate regulatory excellence. This is an opportunity to influence how technology enables better decision-making, stronger collaboration, and lasting impact across the organisation.
Key ResponsibilitiesDrive end-to-end delivery and tracking of the Regulatory Affairs Technology Roadmap portfolio.Maintain portfolio plans, milestones, dependencies, and resource forecasts across multiple workstreams.Partner with technology and business teams to deliver projects on time and within budget.Lead project governance activities, status reviews, and stakeholder communications.Monitor project risks and implement mitigation plans to support successful delivery.Develop clear portfolio reporting, dashboards, and executive-ready updates for leadership.Identify opportunities to enhance processes, project practices, and technology adoption across Regulatory Affairs.Essential RequirementsBachelor’s degree in Computer Science, Life Sciences, or a related discipline.Significant project or portfolio management experience within pharmaceutical, life sciences, or regulated environments.Proven expertise administering Jira or comparable project portfolio management and work-tracking platforms.Strong experience managing project budgets, financial reporting, resource planning, and portfolio governance.Excellent stakeholder management skills with the ability to translate complex information into clear business insights.Demonstrated ability to manage multiple cross-functional projects, identify risks, and drive successful outcomes.Benefits & RewardsAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.Expected Annual Base Salary Range for role: £67,900 to £126,100The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines.Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.Commitment to Diversity and Inclusion / EEO paragraphNovartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.
Job details
How this role compares
Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.
We currently track 243 comparable Manager Regulatory Affairs roles across 67 biopharma companies.
Salary context
77 of 243 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 243 comparable roles
+ 24 more countries
Seniority mix
243 of 243 peers have a known seniority level
Therapeutic area mix
25 of 243 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.